A growing medical device organization in London seeks an experienced Quality / Manufacturing Engineer to join their team. This on-site role focuses on ensuring product quality and compliance with regulations in the manufacturing of high-risk medical devices. Candidates should have a strong background in medical devices, particularly with ISO 13485 and 21 CFR 820. Responsibilities include supporting quality activities, managing issues, and collaborating with suppliers. Ideal for those within a commutable distance from South Kensington.
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